CA2940902C - Polymorphs and solid states of tiacumicin b - Google Patents
Polymorphs and solid states of tiacumicin b Download PDFInfo
- Publication number
- CA2940902C CA2940902C CA2940902A CA2940902A CA2940902C CA 2940902 C CA2940902 C CA 2940902C CA 2940902 A CA2940902 A CA 2940902A CA 2940902 A CA2940902 A CA 2940902A CA 2940902 C CA2940902 C CA 2940902C
- Authority
- CA
- Canada
- Prior art keywords
- tiacumicin
- xrpd
- solvate
- crystal
- intensity
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000007787 solid Substances 0.000 title description 26
- 229930187202 Tiacumicin Natural products 0.000 title description 22
- 239000012453 solvate Substances 0.000 claims abstract description 93
- ZVGNESXIJDCBKN-UUEYKCAUSA-N fidaxomicin Chemical compound O([C@@H]1[C@@H](C)O[C@H]([C@H]([C@H]1O)OC)OCC\1=C/C=C/C[C@H](O)/C(C)=C/[C@@H]([C@H](/C(C)=C/C(/C)=C/C[C@H](OC/1=O)[C@@H](C)O)O[C@H]1[C@H]([C@@H](O)[C@H](OC(=O)C(C)C)C(C)(C)O1)O)CC)C(=O)C1=C(O)C(Cl)=C(O)C(Cl)=C1CC ZVGNESXIJDCBKN-UUEYKCAUSA-N 0.000 claims abstract description 85
- 229960000628 fidaxomicin Drugs 0.000 claims abstract description 85
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 61
- 239000013078 crystal Substances 0.000 claims description 97
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 65
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract description 36
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract description 28
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract description 22
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract description 21
- 229940032007 methylethyl ketone Drugs 0.000 abstract description 12
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 abstract description 9
- 229940011051 isopropyl acetate Drugs 0.000 abstract description 9
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 abstract description 9
- 239000000463 material Substances 0.000 description 35
- 238000003860 storage Methods 0.000 description 20
- 239000002904 solvent Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 16
- 229960004592 isopropanol Drugs 0.000 description 13
- 238000004128 high performance liquid chromatography Methods 0.000 description 10
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- 239000002002 slurry Substances 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- 229940079593 drug Drugs 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000000003 thermogravimetry coupled to Fourier transform infrared spectroscopy Methods 0.000 description 5
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- -1 US8722863 Natural products 0.000 description 3
- 229960000074 biopharmaceutical Drugs 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 150000004677 hydrates Chemical class 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 241000183229 Actinoplanes deccanensis Species 0.000 description 2
- 241001495431 Dactylosporangium aurantiacum Species 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 239000004148 curcumin Substances 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 238000004108 freeze drying Methods 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 102100031480 Dual specificity mitogen-activated protein kinase kinase 1 Human genes 0.000 description 1
- 101710146526 Dual specificity mitogen-activated protein kinase kinase 1 Proteins 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 101150046432 Tril gene Proteins 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000012296 anti-solvent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000036765 blood level Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000004807 desolvation Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 229940088679 drug related substance Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012847 fine chemical Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 230000007773 growth pattern Effects 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461954715P | 2014-03-18 | 2014-03-18 | |
| US61/954,715 | 2014-03-18 | ||
| US201462020570P | 2014-07-03 | 2014-07-03 | |
| US62/020,570 | 2014-07-03 | ||
| PCT/EP2015/055531 WO2015140153A1 (en) | 2014-03-18 | 2015-03-17 | New polymorphs and new solid states of tiacumicin b |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2940902A1 CA2940902A1 (en) | 2015-09-24 |
| CA2940902C true CA2940902C (en) | 2022-10-25 |
Family
ID=52697399
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2940902A Active CA2940902C (en) | 2014-03-18 | 2015-03-17 | Polymorphs and solid states of tiacumicin b |
Country Status (17)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108727387B (zh) * | 2018-07-25 | 2021-03-16 | 天津大学 | 依鲁替尼乙酸异丙酯溶剂化合物及其制备方法 |
| CN109053738B (zh) * | 2018-08-29 | 2020-10-16 | 浙江工业大学 | 一种依鲁替尼的溶剂化物及其制备方法 |
| CN114224899B (zh) * | 2020-09-09 | 2024-04-26 | 首都医科大学附属北京胸科医院 | 非达霉素用于制备抑制脓肿分枝杆菌活性的产品 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4918174A (en) | 1986-09-26 | 1990-04-17 | Abbott Laboratories | Tiacumicin compounds |
| EP1539977B1 (en) | 2002-07-29 | 2014-10-08 | Optimer Pharmaceuticals, Inc. | Tiacumicin production |
| US7378508B2 (en) | 2007-01-22 | 2008-05-27 | Optimer Pharmaceuticals, Inc. | Polymorphic crystalline forms of tiacumicin B |
| KR101203118B1 (ko) * | 2005-01-31 | 2012-11-20 | 옵티머 파마슈티칼즈, 인코포레이티드 | 18-원자 거대고리들 및 그 유사체들 |
| ZA200905337B (en) | 2007-01-22 | 2010-10-27 | Optimer Pharmaceuticals Inc | Macrocyclic polymorphs, compositions comprising such polymorphs, and methods of use and manufacture thereof |
| ITMI20120560A1 (it) | 2012-04-05 | 2013-10-06 | Olon Spa | Procedimento per la purificazione della tiacumicina b |
| US8722863B2 (en) | 2012-05-10 | 2014-05-13 | Teva Pharmaceutical Works Ltd. | Solid state forms of fidaxomycin and processes for preparation thereof |
| CN104768963A (zh) | 2012-05-10 | 2015-07-08 | 特瓦制药厂有限公司 | 非达霉素的固态形式及其制备方法 |
-
2015
- 2015-03-17 WO PCT/EP2015/055531 patent/WO2015140153A1/en not_active Ceased
- 2015-03-17 CA CA2940902A patent/CA2940902C/en active Active
- 2015-03-17 HR HRP20180668TT patent/HRP20180668T1/hr unknown
- 2015-03-17 PT PT157111220T patent/PT3119793T/pt unknown
- 2015-03-17 PL PL15711122T patent/PL3119793T3/pl unknown
- 2015-03-17 US US15/126,347 patent/US10227371B2/en active Active
- 2015-03-17 BR BR112016021542-7A patent/BR112016021542B1/pt active IP Right Grant
- 2015-03-17 SI SI201530241T patent/SI3119793T1/en unknown
- 2015-03-17 KR KR1020167027975A patent/KR20160134719A/ko not_active Ceased
- 2015-03-17 AU AU2015233583A patent/AU2015233583B2/en active Active
- 2015-03-17 HU HUE15711122A patent/HUE038426T2/hu unknown
- 2015-03-17 EP EP15711122.0A patent/EP3119793B1/en active Active
- 2015-03-17 DK DK15711122.0T patent/DK3119793T3/en active
- 2015-03-17 ES ES15711122.0T patent/ES2668351T3/es active Active
- 2015-03-17 CN CN201580013984.XA patent/CN106103462A/zh active Pending
- 2015-03-17 JP JP2016558001A patent/JP2017507994A/ja active Pending
-
2016
- 2016-09-08 IL IL247726A patent/IL247726A0/en unknown
-
2019
- 2019-03-05 IL IL265180A patent/IL265180B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2015233583B2 (en) | 2019-04-11 |
| KR20160134719A (ko) | 2016-11-23 |
| IL265180B (en) | 2022-01-01 |
| JP2017507994A (ja) | 2017-03-23 |
| HRP20180668T1 (hr) | 2018-06-15 |
| CN106103462A (zh) | 2016-11-09 |
| AU2015233583A1 (en) | 2016-09-15 |
| US10227371B2 (en) | 2019-03-12 |
| WO2015140153A1 (en) | 2015-09-24 |
| SI3119793T1 (en) | 2018-06-29 |
| IL247726A0 (en) | 2016-11-30 |
| CA2940902A1 (en) | 2015-09-24 |
| BR112016021542B1 (pt) | 2023-01-31 |
| DK3119793T3 (en) | 2018-05-22 |
| EP3119793B1 (en) | 2018-03-14 |
| US20170081355A1 (en) | 2017-03-23 |
| PL3119793T3 (pl) | 2018-07-31 |
| ES2668351T3 (es) | 2018-05-17 |
| BR112016021542A2 (enrdf_load_stackoverflow) | 2017-08-15 |
| PT3119793T (pt) | 2018-05-10 |
| IL265180A (en) | 2019-05-30 |
| EP3119793A1 (en) | 2017-01-25 |
| HUE038426T2 (hu) | 2018-10-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20200220 |
|
| EEER | Examination request |
Effective date: 20200220 |
|
| EEER | Examination request |
Effective date: 20200220 |